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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 3 |
2009 | 2 |
2024 | 0 |
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5 results
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Page 1
The MCT8 thyroid hormone transporter and Allan-Herndon-Dudley syndrome.
Best Pract Res Clin Endocrinol Metab. 2007 Jun;21(2):307-21. doi: 10.1016/j.beem.2007.03.009.
Best Pract Res Clin Endocrinol Metab. 2007.
PMID: 17574010
Free PMC article.
Review.
The impact of spermine synthase (SMS) mutations on brain morphology.
Kesler SR, Schwartz C, Stevenson RE, Reiss AL.
Kesler SR, et al.
Neurogenetics. 2009 Oct;10(4):299-305. doi: 10.1007/s10048-009-0184-2. Epub 2009 Mar 7.
Neurogenetics. 2009.
PMID: 19277733
Free PMC article.
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Craniofacioskeletal syndrome: an X-linked dominant disorder with early lethality in males.
Stevenson RE, Brasington CK, Skinner C, Simensen RJ, Spence JE, Kesler S, Reiss AL, Schwartz CE.
Stevenson RE, et al.
Am J Med Genet A. 2007 Oct 1;143A(19):2321-9. doi: 10.1002/ajmg.a.31928.
Am J Med Genet A. 2007.
PMID: 17853486
Free PMC article.
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A missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome.
Becerra-Solano LE, Butler J, Castañeda-Cisneros G, McCloskey DE, Wang X, Pegg AE, Schwartz CE, Sánchez-Corona J, García-Ortiz JE.
Becerra-Solano LE, et al.
Am J Med Genet A. 2009 Mar;149A(3):328-35. doi: 10.1002/ajmg.a.32641.
Am J Med Genet A. 2009.
PMID: 19206178
Free PMC article.
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Altered neurodevelopment associated with mutations of RSK2: a morphometric MRI study of Coffin-Lowry syndrome.
Kesler SR, Simensen RJ, Voeller K, Abidi F, Stevenson RE, Schwartz CE, Reiss AL.
Kesler SR, et al.
Neurogenetics. 2007 Apr;8(2):143-7. doi: 10.1007/s10048-007-0080-6. Epub 2007 Feb 22.
Neurogenetics. 2007.
PMID: 17318637
Free PMC article.
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